Referenced in: none

Automatically associated channels: Kv7.1

Title: Disruption of the potassium channel regulatory subunit KCNE2 causes iron-deficient anemia.

Authors: Grace Salsbury, Emma L Cambridge, Zoe McIntyre, Mark J Arends, Natasha A Karp, Christopher Isherwood, Carl Shannon, Yvette Hooks, , Ramiro Ramirez-Solis, David J Adams, Jacqueline K White, Anneliese O Speak

Journal, date & volume: Exp. Hematol., 2014 Dec , 42, 1053-8.e1

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/25127743

Abstract
Iron homeostasis is a dynamic process that is tightly controlled to balance iron uptake, storage, and export. Reduction of dietary iron from the ferric to the ferrous form is required for uptake by solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 (Slc11a2) into the enterocytes. Both processes are proton dependent and have led to the suggestion of the importance of acidic gastric pH for the absorption of dietary iron. Potassium voltage-gated channel subfamily E, member 2 (KCNE2), in combination with potassium voltage-gated channel, KQT-like subfamily, member 1 (KCNQ1), form a gastric potassium channel essential for gastric acidification. Deficiency of either Kcne2 or Kcnq1 results in achlorhydia, gastric hyperplasia, and neoplasia, but the impact on iron absorption has not, to our knowledge, been investigated. Here we report that Kcne2-deficient mice, in addition to the previously reported phenotypes, also present with iron-deficient anemia. Interestingly, impaired function of KCNQ1 results in iron-deficient anemia in Jervell and Lange-Nielsen syndrome patients. We speculate that impaired function of KCNE2 could result in the same clinical phenotype.